chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	130556123	130556124	A	G	60	GENIC	homozygous	115890580
7	130556165	130556166	C	T	63	GENIC	homozygous	115890582
7	130556669	130556670	A	G	38	GENIC	possibly homozygous	115890584
7	130556712	130556713	G	T	43	GENIC	possibly homozygous	115890586
7	130556727	130556728	A	T	41	GENIC	possibly homozygous	115890588
7	130556738	130556739	A	G	41	GENIC	possibly homozygous	115890590
7	130557064	130557065	T	C	47	GENIC	possibly homozygous	115890592
7	130557291	130557292	G	A	48	GENIC	homozygous	115890594
7	130557836	130557837	C	T	57	GENIC	homozygous	115890596
7	130558115	130558116	G		12	GENIC	possibly homozygous	132658277
7	130558123	130558123		A	16	GENIC	possibly homozygous	132658278
7	130558518	130558519	G	A	45	GENIC	homozygous	115890598
7	130558657	130558658	T	C	43	GENIC	homozygous	115890600
7	130558747	130558748	G	T	45	GENIC	homozygous	115890602
7	130558847	130558848	T	C	59	GENIC	homozygous	115890604
7	130559154	130559155	T	C	53	GENIC	homozygous	115890606
7	130559746	130559746		GA	66	GENIC	homozygous	128520362
7	130559962	130559963	A	G	56	GENIC	homozygous	115890608
7	130559993	130559994	C	A	59	GENIC	homozygous	115890609
7	130560530	130560531	A	G	62	GENIC	homozygous	115890611
7	130560735	130560736	G	A	69	GENIC	homozygous	115890613
7	130561146	130561147	A	G	57	GENIC	homozygous	115890615
7	130561298	130561299	G	A	54	GENIC	homozygous	115890619
7	130561671	130561672	T	C	47	GENIC	homozygous	115890621
7	130561781	130561782	C	T	55	GENIC	homozygous	115890623
7	130561970	130561971	T	C	51	GENIC	homozygous	115890625
7	130563831	130563832	G	C	60	GENIC	homozygous	115890627
7	130557418	130557419	C	T	46	GENIC	homozygous	118384655
7	130562238	130562238		CA	37	GENIC	possibly homozygous	132866736
7	130564193	130564194	G	C	56	GENIC	homozygous	115890629
7	130564525	130564526	C	G	54	GENIC	homozygous	118384656